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Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles

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dc.contributor.author Kumar, Indresh
dc.date.accessioned 2021-10-27T04:27:18Z
dc.date.available 2021-10-27T04:27:18Z
dc.date.issued 2019
dc.identifier.uri https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra04741g
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3161
dc.description.abstract An efficient protocol for the synthesis of 2,2-disubstituted indolin-3-ones under mild conditions has been developed. This reaction involves the copper-catalyzed in situ oxidative de-aromatization of 2-arylindoles to indol-3-one, followed by self-dimerization as well as cross-addition with indoles under mild conditions. The result generates a wide variety of C2-tetrasubstituted indolin-3-ones with good to high yields (62–82%). en_US
dc.language.iso en en_US
dc.publisher RSC en_US
dc.subject Chemistry en_US
dc.subject C2-tetrasubstituted en_US
dc.subject Indolin-3-ones en_US
dc.subject Cu-catalyzed en_US
dc.title Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles en_US
dc.type Article en_US


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